Canonical Allele Identifier: CA3064219539

Gene: DDX3Y

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.12919198G= , CM000686.2:g.12919198G=	GRCh38
NC_000024.9:g.15031110G= , CM000686.1:g.15031110G=	GRCh37
NC_000024.8:g.13540504G=	NCBI36
NG_012831.1:g.20092G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004660.5:c.*1076G= MANE Select	NP_004651.2:n.*1076G=
ENST00000336079.8:c.*1076G= MANE Select	ENSP00000336725.3:n.*1076G=
NM_001122665.3:c.*1076G=	NP_001116137.1:n.*1076G=
NM_001302552.2:c.*1076G=	NP_001289481.1:n.*1076G=
NM_001302552.3:c.*1076G=	NP_001289481.1:n.*1076G=
NM_001324195.1:c.*1076G=	NP_001311124.1:n.*1076G=
NM_001324195.2:c.*1076G=	NP_001311124.1:n.*1076G=
NM_004660.4:c.*1076G=	NP_004651.2:n.*1076G=
NR_136716.1:n.3528G=
NR_136716.2:n.3446G=
NR_136717.1:n.3290G=
NR_136717.2:n.3208G=
NR_136718.1:n.3608G=
NR_136718.2:n.3526G=
NR_136719.1:n.3398G=
NR_136719.2:n.3316G=
NR_136720.1:n.3459G=
NR_136720.2:n.3377G=
NR_136721.1:n.3121G=
NR_136721.2:n.3111G=
NR_136722.1:n.3205G=
NR_136723.1:n.3523G=
NR_136724.1:n.3443G=
ENST00000336079.7:c.*1076G=	ENSP00000336725.3:n.*1076G=
XM_006724878.1:c.*1076G=	XP_006724941.1:n.*1076G=
XR_001756014.2:n.3223G=